Job Openings at UnoCasa Limited

Description 

• Our client is seeking a creative Marketing Services Manager to develop, manage, and execute marketing and sales communication plans for the company’s corporate and product brands.
• This role will align with the Head of Department’s directives to ensure effective marketing strategies and communication initiatives.

Key Responsibilities

• Collaborate with the Head of Department to implement a comprehensive communications strategy.
• Develop, manage, and enhance packaging materials for new and existing products.
• Lead the development of communication materials, marketing tools, and services.
• Supervise, coordinate, and direct the workflow of marketing, advertising, or public relations specialists/agencies.
• Strategically plan and manage annual marketing activities and corresponding budgets.
• Stay updated on competition activities and proactively initiate innovative ideas ahead of competitors.
• Manage and support relevant market activations and events.
• Design and implement digital marketing strategies for consistent digital presence across social media channels.
• Provide support to all company departments as needed.
• Perform other duties and projects as assigned by the Pharma Operations Director or Business Development and Licensing Director.

Educational Qualifications

• Bachelor’s Degree in Business Administration or marketing
• minimum of 6 years of experience in advertising and integrated marketing communications.
• Proficiency in computer usage.
• Strong analytical, meticulous, and problem-solving skills.
• Team player.

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Description 

• Our client is a dedicated pharmaceutical company seeking a Regulatory Affairs Officer to ensure full compliance with regulatory requirements and provide crucial support in the planning and coordination of regulatory activities.

Key Responsibilities

• Gather information and documents for new product registrations, formula changes, and variations in existing products. Submit these to NAFDAC and other relevant authorities for approval.
• Monitor product registrations and ensure timely renewal of existing product approvals.
• Compile product dossiers received from manufacturers in formats acceptable to regulatory agencies.
• Assist in preparing and submitting regulatory agency applications, reports, and correspondence.
• Contribute to the development of regulatory strategies and implementation plans for new product submissions.
• Handle online applications for API permits, Excipient permits, Narcotic permits, and other relevant permits in the single trade portal.
• Support in coordinating and monitoring clinical studies of the company’s products.
• Keep other company departments informed about regulatory requirements.
• Ensure timely submissions and approvals of applications according to regulatory plans and strategies.
• Review marketing materials, information leaflets, and packaging artworks to meet regulatory agency requirements.
• Ensure regulatory compliance in advertisements and secure approval for planned promotional materials.
• Communicate regulatory issues with the Regulatory Affairs Manager and other related departments, formulating appropriate responses.
• Assist in audits, regulatory agency inspections, and product recalls.
• Assist in coordinating the destruction of expired and rejected products and materials.
• Document reported Adverse Drug Reactions and enforce pharmacovigilance compliance related to assigned products.
• Support documentation efforts to ensure compliance with domestic and international regulations and standards.
• Register company premises, Superintendent Pharmacist, and key Organizational Managers with the Pharmacists Council of Nigeria (PCN).
• Represent the department in QMS and cGMP activities.
• Coordinate QMS and cGMP documentation, implementation, and audit-related activities within the department.
• Disseminate information on QMS and cGMP implementation to department staff.
• Complete Corrective Action and Preventive Action Plans for gaps identified during inspections and ensure their closure.
• Provide assistance to external auditors in compliance reviews.
• Participate in internal audits, contribute to report writing, and make presentations at monthly meetings as needed.

Requirements

•  Interested candidates should possess a Bachelor's Degree in relevant fields with 0 - 3 years work experience.

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Description 

• Our client is seeking an experienced Production Manager to ensure that production and manufacturing operations adhere to the highest standards, including WHO GMP, National Regulatory Authority Standards (NAFDAC, PCN, Federal Ministry of Labour and Productivity), and NIS ISO 9001:2008.
• This role plays a pivotal part in ensuring product availability, quality, and meeting sales, marketing, and contract manufacturer requirements.

Key Responsibilities

• Ensuring pharmaceutical products are manufactured and packaged in compliance with WHO Good Manufacturing Practices, ISO standards, and national regulatory authorities.
• Meeting WHO and national guidelines for product quality.
• Coordinating supply chain activities to prevent stock-outs of locally manufactured products.
• Optimizing technical services and capacity utilization while managing costs.
• Overseeing routine maintenance of facilities and machinery for quality and safety.
• Managing personnel, including recruitment, training, and documentation of production processes.
• Establishing documentation systems in line with GMP and occupational health and safety standards.
• Conducting internal GMP audits and validation of manufacturing processes and equipment.
• Leading new projects for product development and reformulation.
• Ensuring compliance with GMP guidelines, national regulations, ISO standards, and company policies.
• Investigating deviations in manufacturing and packaging operations.
• Maintaining discipline and adherence to company-wide policies within the production section.
• Developing and overseeing toll manufacturing operations.
• Recommending equipment upgrades and replacements.
• Collecting and analysing production data to assess manufacturing system efficiency.

Requirements

• Interested candidates should possess a Bachelor's Degree or Master's Degree in relevant fields with a minimum of 12 years work experience.

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Description

• Our client, a pharmaceutical company is dedicated to excellence and compliance, is seeking a Regulatory Affairs Manager to ensure the company’s adherence to regulatory standards, particularly those set by NAFDAC and the Pharmacist Council of Nigeria.

Key Responsibilities

• Maintain the company’s current registration with the Pharmacist Council of Nigeria.
• Lead the preparation and submission of regulatory agency applications, reports, and correspondence.
• Develop and execute regulatory strategies for new product submissions and renewals.
• Respond to regulatory agencies regarding product information and issues.
• Ensure the timeliness, accuracy, and compliance of all regulatory agency submission materials.
• Verify that detailing materials, information leaflets, and packaging artworks meet regulatory requirements.
• Communicate regulatory issues to management and stakeholders and develop appropriate responses.
• Collaborate with all company departments to secure relevant permits and certificates.
• Manage activities such as audits, regulatory agency inspections, and product recalls.
• Coordinate the disposal of expired and rejected products and materials.
• Participate in the development and implementation of clinical trial protocols.
• Provide regulatory guidance to departments and development project teams.
• Oversee documentation efforts to ensure compliance with domestic and international regulations and standards.
• Represent the company in relevant Trade association meetings, including NIROPHARM and PMGMAN.
• Perform any other duties delegated by the line manager.

Requirements

• Interested candidates should possess a Bacheor's Degree in relevant fields with a minimum of 8 years work experience.